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截瘫小鼠正引领着脊髓损伤研究取得新进展。

Paraplegic mice are leading to new advances in spinal cord injury research.

作者信息

Guertin P A

机构信息

Department of Anatomy and Physiology, Laval University, Quebec, Canada.

出版信息

Spinal Cord. 2005 Aug;43(8):459-61. doi: 10.1038/sj.sc.3101754.

Abstract

STUDY DESIGN

Experimental laboratory investigations with paraplegic mouse models.

OBJECTIVES

To review the most recent advances in the field of spinal cord injury research; immune system response, regeneration, and functional recovery.

SETTINGS

Laval University and Laval University Medical Center, Quebec, Canada.

METHODS

Assessment of regenerative processes and locomotor function recovery induced by a variety of treatments and approaches in wild-type and genetically engineered mice with complete or incomplete lesions of the spinal cord.

RESULTS

Recent studies have reported a number of significant observations providing additional insight into the role and mechanism of regeneration, immune system response, and functional recovery after spinal cord injury (SCI) using incomplete paraplegic mice with Nogo-A, NgR, EphA4, GFAP/vimentime, LIF, or Fas gene knock-out. A novel antibody called CXCL10 was also recently found to increase tissue sparing and angiogenesis after SCI. In an attempt to explore the possibilities of reactivating spared neurons below the injury level, researchers have found that pharmacological activation of specific subtypes of serotonin receptors (eg, 5-HT1A/2A/7) can sustain the production of basic locomotor-like movements in complete paraplegic mice.

CONCLUSION

The growing availability of genetically engineered and mutant mouse strains along with molecular biology tools has led scientists to increasingly use murine models in SCI research. These new tools and models may assist scientists in understanding further the complex pathological consequences of SCI.

摘要

研究设计

使用截瘫小鼠模型进行实验性实验室研究。

目的

回顾脊髓损伤研究领域的最新进展;免疫系统反应、再生和功能恢复。

地点

加拿大魁北克省拉瓦尔大学和拉瓦尔大学医学中心。

方法

评估在野生型和基因工程小鼠中,各种治疗方法和途径对脊髓完全或不完全损伤后再生过程和运动功能恢复的影响。

结果

最近的研究报告了一些重要发现,这些发现通过使用Nogo-A、NgR、EphA4、GFAP/波形蛋白、LIF或Fas基因敲除的不完全截瘫小鼠,为脊髓损伤(SCI)后再生、免疫系统反应和功能恢复的作用及机制提供了更多见解。最近还发现一种名为CXCL10的新型抗体可增加SCI后的组织保留和血管生成。为了探索激活损伤水平以下备用神经元的可能性,研究人员发现,对特定亚型的血清素受体(如5-HT1A/2A/7)进行药理学激活,可以维持完全截瘫小鼠基本的类似运动的动作产生。

结论

基因工程和突变小鼠品系以及分子生物学工具的日益普及,促使科学家们在SCI研究中越来越多地使用小鼠模型。这些新工具和模型可能有助于科学家进一步了解SCI的复杂病理后果。

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